Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_provenance.
- NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_assertion description "[Based on the previous finding that mutations in COL3A1 cause type IV EDS, our study indicates a possible common pathological pathway linking connective tissue diseases and brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_provenance.
- NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_assertion evidence source_evidence_literature NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_provenance.
- NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_assertion SIO_000772 22235340 NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_provenance.
- NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_assertion wasDerivedFrom befree-20140225 NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_provenance.
- NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_assertion wasGeneratedBy ECO_0000203 NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP768014.RAFKm1CifOYqQZO0DfxYAu2WERU7AQinmvh0IsoM2YJN4130_provenance.